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Our client is seeking a dynamic and experienced leader to join their team as the Leader of Quality Control. In this role, you will be responsible for overseeing and driving the Quality Control function within the organization.
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A minimum of 10 years in similar cGMP environments with broad knowledge of Quality Control procedures, bioanalytical, chemistry, microbiology assays for sterility, endotoxin, TOC, and stability programs required for biologic therapies.
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Responsible for directing the Quality Control Department objectives aimed at continuous improvement and strict adherence to cGMP guidelines, maintaining knowledge of new guidance as applicable.
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Our R&D Quality Control team seeks a talented Senior QC Analytical Chemist to join an innovative organization to serve as Cresilon's Subject Matter Expert (SME) and technical leader in cGMP Analytical Chemistry.
$110,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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Establishes and executes development project plans (e.g., process and assay development, assay qualification, support tech transfer of processes) from cGMP manufacturing and assays to quality control.
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Job Title: Quality Control Lab - Quality Control Chemist (QCL- QC. Chemist) Quality Control Lab Manager. Quality Control and Troubleshooting:Identify potential quality issues, deviations, or non-conformities during testing processes and work collaboratively with the Quality Control team to address and rectify them.
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Working cross functionally with Analytical Development, Process Development, Manufacturing, MSAT, Regulatory, and Quality Assurance departments. Project involvement will start with cGMP lab infrastructure and operation needs and will continue through method transfer, verification and/ or validations, on to routine analysis of cGMP starting materials, in-process samples, and release testing of cGMP pharmaceutical products.
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We seek a Quality Control (QC) EM Specialist to support the Pilot Bioproduction Facility (PBF) at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland. PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies.
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The Associate Director, Quality Control (Viral Vector) is responsible for managing the Quality Control Viral Vector team and testing operations to support GMP Cell and Gene Therapy Manufacturing.
$133,550 - $163,228 a yearFull-timeExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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Familiarity with cGMP Quality Control Testing, Qualification, and validation of analytical test methods compliant to Good Laboratory and Documentation Practices. Supervise QC analyst(s) Responsible for QC data/records to ensure content adheres to established cGMP quality standards.
$150,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated 0 days ago - UpvoteDownvoteShare Job
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Este rol requiere tenacidad, una sólida comprensión de las prácticas de control de calidad, los fundamentos de la seguridad alimentaria, la resolución de problemas, el pensamiento crítico y un enfoque de trabajo en equipo.
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Reporting to the Senior Manager of ADQC, the primary role of the Scientist I in Analytical Development/Quality Control (ADQC) is to provide support to clinical programs by providing quality testing and delivering results in accordance with cGMP standards.
$128,000 - $149,000 a yearFull-timeExpandApply NowActive JobUpdated 36 days ago - UpvoteDownvoteShare Job
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Quality control sample management experience in the pharmaceutical industry supporting cGMP areas preferred. The QC Sample Management Consultant position will be responsible for supporting the Quality Control team in the establishment of a robust GMP sample shipment process as well as internal sample tracking/reporting capabilities.
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Quality Control Scientist IV , demonstrates full understanding of scientific and technical aspects of biological Drug Product/ Drug Substance (DP/DS), as well as technology transfer, assay qualifications and validations activities.
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We are seeking an experienced Quality Control Production Associate who will be responsible for managing and expanding OBX's quality assurance program which includes: industry, regulatory, and cGMP manufacturing compliance and certification programs; in-house and third party product quality testing throughout the manufacturing process; and comprehensive SOP's and employee compliance training.
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